Suzaki Takuya, Ohneda Masako, Toriba Taiyo, Yoshida Akiko, Hirano Hiro-Yuki
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Bunkyo-ku, Tokyo, Japan.
PLoS Genet. 2009 Oct;5(10):e1000693. doi: 10.1371/journal.pgen.1000693. Epub 2009 Oct 16.
CLAVATA signaling restricts stem cell identity in the shoot apical meristem (SAM) in Arabidopsis thaliana. In rice (Oryza sativa), FLORAL ORGAN NUMBER2 (FON2), closely related to CLV3, is involved as a signaling molecule in a similar pathway to negatively regulate stem cell proliferation in the floral meristem (FM). Here we show that the FON2 SPARE1 (FOS1) gene encoding a CLE protein functions along with FON2 in maintenance of the FM. In addition, FOS1 appears to be involved in maintenance of the SAM in the vegetative phase, because constitutive expression of FOS1 caused termination of the vegetative SAM. Genetic analysis revealed that FOS1 does not need FON1, the putative receptor of FON2, for its action, suggesting that FOS1 and FON2 may function in meristem maintenance as signaling molecules in independent pathways. Initially, we identified FOS1 as a suppressor that originates from O. sativa indica and suppresses the fon2 mutation in O. sativa japonica. FOS1 function in japonica appears to be compromised by a functional nucleotide polymorphism (FNP) at the putative processing site of the signal peptide. Sequence comparison of FOS1 in about 150 domesticated rice and wild rice species indicates that this FNP is present only in japonica, suggesting that redundant regulation by FOS1 and FON2 is commonplace in species in the Oryza genus. Distribution of the FNP also suggests that this mutation may have occurred during the divergence of japonica from its wild ancestor. Stem cell maintenance may be regulated by at least three negative pathways in rice, and each pathway may contribute differently to this regulation depending on the type of the meristem. This situation contrasts with that in Arabidopsis, where CLV signaling is the major single pathway in all meristems.
CLAVATA信号通路限制了拟南芥茎尖分生组织(SAM)中的干细胞特性。在水稻(Oryza sativa)中,与CLV3密切相关的花器官数量2(FON2)作为信号分子参与了一条类似的通路,对花分生组织(FM)中的干细胞增殖起负调控作用。在此,我们表明编码CLE蛋白的FON2 SPARE1(FOS1)基因与FON2共同作用维持FM。此外,FOS1似乎还参与营养生长阶段SAM的维持,因为FOS1的组成型表达导致营养生长SAM的终止。遗传分析表明,FOS1发挥作用不需要FON1(FON2的假定受体),这表明FOS1和FON2可能作为独立通路中的信号分子在分生组织维持中发挥作用。最初,我们将FOS1鉴定为一个源自籼稻的抑制子,它能抑制粳稻中的fon2突变。粳稻中FOS1的功能似乎因信号肽假定加工位点的一个功能性核苷酸多态性(FNP)而受损。对约150个驯化水稻和野生稻品种的FOS1序列比较表明,这种FNP仅存在于粳稻中,这表明FOS1和FON2的冗余调控在稻属物种中很常见。FNP的分布还表明,这种突变可能发生在粳稻与其野生祖先分化的过程中。水稻中的干细胞维持可能由至少三条负调控通路调节,并且每条通路可能根据分生组织的类型对这种调节有不同的贡献。这种情况与拟南芥不同,在拟南芥中CLV信号通路是所有分生组织中的主要单一通路。